Canonical Allele Identifier: CA459008425

Gene: VIPR2

Linked Data

• MyVariant Identifiers: chr7:g.158827314C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034623C>T , CM000669.2:g.159034623C>T	GRCh38
NC_000007.13:g.158827314C>T , CM000669.1:g.158827314C>T	GRCh37
NC_000007.12:g.158520075C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.837G>A MANE Select	ENSP00000262178.2:p.Val279=
ENST00000262178.6:c.837G>A	ENSP00000262178.2:p.Val279=
ENST00000377633.7:c.789G>A	ENSP00000366860.3:p.Val263=
ENST00000402066.5:c.1260G>A	ENSP00000384497.1:p.Val420=
NM_001304522.1:c.597G>A	NP_001291451.1:p.Val199=
NM_001308259.1:c.789G>A	NP_001295188.1:p.Val263=
NM_003382.4:c.837G>A	NP_003373.2:p.Val279=
NR_130758.1:n.1023G>A
XM_005249561.2:c.912G>A	XP_005249618.1:p.Val304=
XM_006716107.1:c.837G>A	XP_006716170.1:p.Val279=
XM_006716108.2:c.648G>A	XP_006716171.1:p.Val216=
XM_011516550.1:c.789G>A	XP_011514852.1:p.Val263=
XM_011516552.1:c.423G>A	XP_011514854.1:p.Val141=
XR_242047.2:n.1232G>A
XM_005249561.3:c.912G>A	XP_005249618.1:p.Val304=
XM_006716107.2:c.837G>A	XP_006716170.1:p.Val279=
XM_006716108.3:c.648G>A	XP_006716171.1:p.Val216=
XM_011516550.2:c.789G>A	XP_011514852.1:p.Val263=
XM_017012580.1:c.423G>A	XP_016868069.1:p.Val141=
XM_024446914.1:c.912G>A	XP_024302682.1:p.Val304=
XM_024446915.1:c.912G>A	XP_024302683.1:p.Val304=
XM_024446916.1:c.837G>A	XP_024302684.1:p.Val279=
XM_024446917.1:c.648G>A	XP_024302685.1:p.Val216=
XM_024446918.1:c.423G>A	XP_024302686.1:p.Val141=
NM_003382.5:c.837G>A MANE Select	NP_003373.2:p.Val279=
NM_001304522.2:c.597G>A	NP_001291451.1:p.Val199=
NR_130758.2:n.933G>A